WormBase Tree Display for Variation: WBVar01719612

WBVar01719612 Name: Public_name: WBVar01719612
    Other_name: cewivar00417731
      F10G7.10.1:c.5565C>T
      CE54007:p.Asn1855=
      F10G7.10.2:c.5565C>T
    HGVSg: CHROMOSOME_II:g.4718551G>A
  Sequence_details: SMap: S_parent: Sequence: F41C3
    Flanking_sequences: AACACTTACAATTCTCTTCAACTTCGCCAT TTCGTCAACTGAGTTCTGAAGGCTCTCGTC
    Mapping_target: F41C3
    Source_location: 225 CHROMOSOME_II 4718548 4718548 From_analysis: Million_mutation_project_reanalysis
    Type_of_mutation: Substitution: G A
    SeqStatus: Sequenced
  Variation_type: Natural_variant
  Origin: Species: Caenorhabditis elegans
    Strain: WBStrain00023139 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027648 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027660 From_analysis: Million_mutation_project_reanalysis
      WBStrain00027662 From_analysis: Million_mutation_project_reanalysis
    Laboratory: VC
    Analysis: Million_mutation_project_reanalysis
    Status: Live
  Affects: Gene: WBGene00017373
    Transcript: F10G7.10.1 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F10G7.10.1:c.5565C>T
        HGVSp: CE54007:p.Asn1855=
        cDNA_position: 5587
        CDS_position: 5565
        Protein_position: 1855
        Exon_number: 21/25
        Codon_change: aaC/aaT
        Amino_acid_change: N
      F10G7.10.2 VEP_consequence: synonymous_variant
        VEP_impact: LOW
        HGVSc: F10G7.10.2:c.5565C>T
        HGVSp: CE54007:p.Asn1855=
        cDNA_position: 5638
        CDS_position: 5565
        Protein_position: 1855
        Exon_number: 22/26
        Codon_change: aaC/aaT
        Amino_acid_change: N
  Method: WGS_Flibotte